Job Description Working hours are Monday Friday, working 37hrs flexibly between 7am - 7pm. The purpose of this job within Analytical Science is to support the client in both Manufacturing and R&D efforts by conducting analysis and characterization of the samples generated. Main Duties Support formulation development through hands-on generation of accurate and precise analytical chemistry data using routine laboratory techniques. Design and execution of studies to ascertain degradation mechanisms in the solution and solid state. Assess stability risks by evaluating process changes and impact on degradation chemistry or dissolution profile. Development of assay/purity methods and assessment of method robustness/ruggedness Development and execution of method validation protocols. Transfer of analytical methods to other laboratories and remote sites. Hands-on generation of data in support of accelerated and registration stability studies. Development and support of Process Analytical Technology (PAT) techniques. Demonstrate understanding of root cause analysis methodologies and be able to support investigations as required. Demonstrate an understanding in the analyses required in the formulation of amorphous dispersions. Report and communicate project outcomes in an appropriate manner. Identify and resolve promptly any problems occurring at any phase of a study, escalating to the line manager where necessary. Ensure all applicable quality measures are met and adhered to. To keep an accurate up to date laboratory notebook including interpretation or results, conclusions and next steps To collect and measure productivity through agreed metrics such as number of tests performed, cycle times, lab/product issues, number of hours worked per project, etc. Ensure that the client gets the best possible service by continually reviewing best practice in relation to both commercial and quality issues and ensuring 100% ethical work standards. To become fully familiar with and keep up to date with any technological or method revisions in their area. To keep the laboratory area clean and tidy in both ‘seen’ and ‘unseen’ areas. To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards. To update any relevant documentation when requested.